The University IRB applies all Department of Health and Human Services (DHHS) requirements for informed consent to greater than minimal risk research: DHHS general requirements (at 45 CFR 46.116) (see ...

Obtaining informed consent is a basic ethical obligation and a legal requirement for researchers. This requirement is founded on the principle of respect for persons. Potential participants must be ...

Informed consent (IC) is a fundamental aspect of ethical clinical research, safeguarding the rights and well-being of participants. It empowers participants with comprehensive information about the ...

The Forms and Templates page includes templates for informed consent documents.. However, because each human participants research (HSR) proposal is different and carries unique risks to participants, ...

All protocols must detail the informed consent process personnel will use if participants will be involved in the research study. Protocols must use the W&M-approved Informed Consent Form (ICF) linked ...

Key features of informed consent include disclosure of all details about the trial—from how far a subject may need to travel to get to a research site to potential side effects—as well as ...

A day after suspending its study of the use of ketamine on agitated people by paramedics, Hennepin Healthcare said it would halt similar clinical trials that seek consent from patients only after ...